NZ500143A

NZ500143A - 6-(substituted phenyl)-7-trifluoroalkylamino-[1,2,4]triazolo[1,5-a]pyrimidine derivatives, fungicidal compositions and a method of combating phytopathogenic fungi

Info

Publication number: NZ500143A
Application number: NZ500143A
Authority: NZ
Inventors: Leslie May; Waldemar Pfrengle; Guido Albert; Klaus-Juergen Pees; Guenter Krummel; Henry Van Tuyl Cotter; Annerose Rehnig
Original assignee: American Cyanamid Co
Priority date: 1997-04-14
Filing date: 1998-03-23
Publication date: 2001-06-29
Also published as: DK0945453T3; EA002906B1; BG64197B1; SK283232B6; NO313416B1; AU735730B2; NO994973L; CN1257502A; DE69903988D1; NO994973D0; TR199902552T2; CA2287470A1; HUP0001993A2; ID24182A; ES2199436T3; TW460476B; CZ359699A3; ATE228133T1; EE04373B1; RS49776B

Abstract

The compound (useful as a herbicide) has the general formula I, wherein: R1 and R2 each independently represent H or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl or phenyl group. Hal represents a halogen atom L1, L2, L3, L4 and L5 each independently represent H, halogen, alkyl, alkoxy or nitro. alkyl, alkenyl, alkynyl and alkadienyl refer to straight or branched chain radicals or moieties having up to 10 carbon atoms each optionally substituted group independently is substituted by one or more halogen atoms or nitro, cyano, alkyl, cycloalkyl, cycloalkenyl, haloalkyl, halocycloalkyl, alkoxy, haloalkoxy, trialkylsilyl, phenyl, halo- or dihalo-phenyl or pyridyl groups. A process for the preparation of the compounds of formula I is also described. Also described are fungicidal compositions which comprise a carrier, and at least one compound of formula I. Also described is a method of combating phytopathogenic fungus at a locus which comprises treating the locus with a compound of formula I.

Description

<div class="application article clearfix" id="description"> WO 98/46608 PCT/US98/0S615 FUNGICIDAL TRIFLUOROMETHYLALKYLAMINO-TRIAZOLOPYR1MIDINES BACKGROUND OF THE INVENTION This invention relates to certain triazolopyrimidine compounds, a process for their preparation, compositions containing such compounds, a method for combating a fungus at a locus comprising treating the locus with such compounds 5 and their use as fungicides EP-A-0 071 792 claims compounds of the general formula in which R1 represents alkyl, halogen, aikoxy, cyano, cycloalkyl, aryl, aryloxy, arylthio, aralkyl, arylthio, arylaikyl, arylalkyloxy or arylalkylthio each optionally 10 substituted by halogen or aikoxy; or (R1)n represents a benzene, indane or tetrahydronaphthalene ring fused with the phenyl ring, aromatic moieties in the above groups being optionally substituted by alkyl, aikoxy, halogen or cyano; n is 1 or 2, R2 and R3 are each hydrogen, alkyl or aryl, A represents a nitrogen atom or a CR4group, and R4 is as R2 but can also be halogen, cyano or alkoxycarbonyl or 15 together with R3 can form an alkylene chain containing up to two double bonds The compounds are said to be active against various phytopathogenic fungi, especially those of the phycomycete class However evide^y of fungicidal activity is only provided for these compounds against Plasmopara viticola, a member of the oomycete class of fungi. 20 EP 0 550 113-A2 claims compounds of the general formula SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 2 PCT/US98/05615 in which R1 represents an optionally substituted alkyl, alkenyl, alkadienyl, cycloalkyi, bicycloalkyi or heterocyclyl group; R2 represents a hydrogen atom or an alkyl group; or R1 and R2 together with the interjacent nitrogen atom represent an 5 optionally substituted heterocyclic ring; R3 represents an optionally substituted aryl group; and R" represents a hydrogen or halogen atom or a group -NR5R6 where R5 represents a hydrogen atom or an amino, alkyl, cycloalkyi or bicycloalkyi group and R6 represents a hydrogen atom or an alkyl group Thus, compounds in which R1 is a trifluoromethylalkyl group are generally embraced by this patent 10 application However, there is no single compound disclosed in which R1 is a trifluoromethylalkyl group SUBSTITUTE SHEET (RULE 26) Printed from Mimosa L -3- (fol lowed by page 3a) SUMMARY OF THE INVENTION In a first aspect, the present invention provides a compound of formula I in which R1 and R2 each independently represent a hydrogen atom or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl or phenyl group, Hal represents a halogen atom, L1 through L5each independently represent an hydrogen or halogen atom or an alkyl, aikoxy or nitro group in which the terms alkyl, alkenyl, alkynyl alkadienyl refer to straight or branched chain radicals or moieties having up to 10 carbon atoms; in which each optionally substituted group independently is substituted by one or more halogen atoms or nitro, cyano, alkyl, cycloalkyi, cycloalkenyl, haloalkyl, halocycloalkyl, aikoxy, haloalkoxy, trialkylsilyl, phenyl, halo- or dihalo-phenyi or pyridyl groups. The new compounds show an excellent selective fungicidal activity in various crops. In a further aspect, the present invention provides a process for the preparation of a compound of formula I as defined above which comprises treating a compound of the general formula II L' INTELLECTUAL PROPERTY OFFICE OF NZ. RECEIVED 2 5 MAY 2001 Hal L L 4 (II) (followed by page 4) in which L1 through Ls and Hal are as defined above; with an amine of the general formula III M N-R2 (III) F,C—CH V in which R1 and R2 are as defined above, M represents a hydrogen atom or a free or complexed metal atom, to produce a compound of formula I. In a yet further aspect, the present invention provides a fungicidal composition which comprises a carrier, and as active agent, at least one compound of formula I. In a still further aspect, the present invention provides a method of combating phytopathogenic fungus at a locus which comprises treating the locus with a compound of formula I or with a composition as defined above. In another aspect, the present invention provides the use as a fungicide of a compound of formula I or a composition as defined above. Objects of the present invention are. to provide novel, selective fungicidal compounds, to provide methods for controlling undesired fungus by contacting said plants with a fungicidally effective amount of the new compounds, to provide selective fungicidal compositions containing the new compounds as active ingredients; or at least to provide the public with a useful choice. These and other objects and features of the invention will be more apparent from the detailed description set forth hereinbelow, and from the app 'property" OFFICE OF N.Z. - 9 FEB 2001 RECEIVED WO 98/46608 PCT/US98/0561S 4 DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS ' It has surprisingly been found that the novel compounds of formula I L2 <' n (I) n n Hal 5 in which R\ R2, Hal and L1 through L5 have the meaning given above for formula I show an excellent fungicidal activity against a broad range of fungi. In general terms, unless otherwise stated, as used herein the term halogen atom may denote a bromine, iodine, chlorine or fluorine atom, and is especially a bromine, chlorine or fluorine atom. 10 Hal represents preferably fluorine, chlorine, bromine or iodine, in particular Optionally substituted moieties may be unsubstituted or have from one up to the maximal possible number of substituents. Typically, 0 to 3 substituents are present. alkynyl, alkadienyl as used herein with respect to a radical or moiety refer to a straight or branched chain radical or moiety As a rule, such radicals have up to 10, in particular up to 6 carbon atoms. Suitably an alkyl moiety has from 1 to 6 carbon atoms, preferably from 1 to 3 carbon atoms A preferred alkyl moiety is an 20 ethyl or especially a methyl group Suitably an alkenyl moiety has from 2 to 6 carbon atoms. A preferred alkenyl moiety is allyl or especially a 2-methylallyl The invention especially relates to compounds of the general formula I in which any alkyl part of the groups R1 and/or R2 which may be straight chained or 25 branched, contains up to 10 carbon atoms, preferably up to 9 carbon atoms, more preferably up to 6 carbon atoms, any alkenyl or alkynyl part of the substituents R1 and/or R2 contains up to 10 carbon atoms, preferably up to 9 carbon atoms, more preferably up to 6 carbon atoms, and in which each optionally substituted group chlonne. 15 In general terms, unless otherwise stated herein, the terms alkyl, alkenyl, group SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 5 independently is substituted by one or more halogen atoms or nitro, cyano, cycloalkyi, preferably C3< cycloalkyi, cycloalkenyl, preferably CM cycloalkenyl, haloalkyl, preferably haloalkyl, halocycloalkyl, preferably C3.6 halocycloalkyl, aikoxy, preferably C,^ aikoxy, haloalkoxy, preferably C,.6 haloalkoxy, trialkylsilyl, 5 preferably tri-C,., alkylsilyl, phenyl, halo- or dihalo-phenyl or pyridyl groups Any alkyl, alkenyl or alkynyl group may be linear or branched A halogen atom suitably denotes a fluonne, chlorine or bromine atom. The invention especially relates to compounds of the general formula I, in which R1 represents a hydrogen atom, a C.,.10 alkyl or a phenyl group, in particular 10 a hydrogen atom or a methyl group. Included in the scope of the present invention are (R) and (S) isomers and atropisomers of compounds of general formula I, which have a chiral center or in which the substituents L1 or L1 and L2 are different from L5 or L5 and L4, and the racemates thereof, and salts, N-oxides and acid addition compounds. 15 Particularly interesting activity has been found in (S)-isomer compounds of general formula I wherein the group -CH(CF3)R1 is chiral Another preferred embodiment of the present invention are the compounds of formula I, wherein R2 represents a hydrogen atom or a C,.10 alkyl group or a C3. alkenyl group. 20 Those compounds of formula I in which at least one of R1 and R2 represents a hydrogen atom are particularly preferred Particularly preferred are compounds of formula I, in which the phenyl group SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 is selected from The compounds according to general formula I are oils, gums, or, predominantly crystalline solid materials. They are supenor through their valuable fungicidal properties, in particular their enhanced systemicity and enhanced 5 fungicitoxity against rice diseases and powdery mildews. For example, they can be used in agriculture or related fields for the control of phytopathogenic fungi such as Alternana solani, Botrytis cmerea, Cercospora beticola, Cladosponum herbarum, Corticium rolfsii, Erysiphe graminis, Helminthosponum tntici repentis, Leptosphaena nodorum, Micronectriella nivalis, Monihnia fructigena, Myco-10 sphaerella hguhcola, Mycosphaerella pinodes, Pynculana gnsea fsp oryzae, Rhizoctonia solani, Ventuna inaequahs, Uncmula necator and Sclerotinia sclero-tiorum, in particular for the control of Uncmula necator, Pynculana gnsea f.sp oryzae and Rhizoctonia solani. The compounds of general formula I according to the invention possess a high fungicidal activity within a wide concentration range 15 and may be used in agriculture without any difficulties Moreover, the compounds according to the invention show enhanced residual control of fungi, in particular of grape powdery mildew compared with conventional fungicides Good results in terms of control of phythopathogenic fungi are obtained 20 with a compound as defined in formula I wherein. at least one of L1 and L5 represents a halogen atom; and/or SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 7 R1 represents a hydrogen atom or a methyl group. Especially good results in terms of control of phytopathogenic fungi are obtained by using, for example, the following compounds of formula I: 5-chloro-6-(2-chloro-6-fluorophenyl)-7-(2,2,2-tnfluoroethylamino)-5 [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-(2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-7-(2,2,2-tri-fluoroethylamino)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pynmidine, 5-chloro-6-(2-chlorophenyl)-7-(2,2,2-trifluoroethylanninoH1,2,4]tri-azolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-(2,2,2-trifluoro-ethylamino)-10 [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[2-(1,1,1-tnfluoro)propylamino]-[1,2,4]tnazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[2-(1,1,1-trifluoro)propylaminoH1,2,4|triazolo[1,5-a]pyrimidine, 5-chloro-6-(2l4,6-trifluorophenyl)-7-[2-(1,1,1-trifluoro)propylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-methylphenyl)-7-[2-(1,1,1-15 tnfluoro)propylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-[2-(1,1,1-trifluoro)propylamino]-[1l2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chlorophenyl)-7-[2-(1,1,1-trifluoro)propylaminoH1.2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-trifluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[N-(2,2,2-20 trifluoroethyl)-N-allylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylamino]-[1,2,4]tnazolo[1,5-aJpyrimidine, 5-chloro-6-(2-chlorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylamino]-25 [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-methylphenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-30 tnfluorophenyl)-7-[N-(2,2,2-tnfluoroethyl)-N-ethylamino]- [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chlorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethylamino]- SUBST1TUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 8 [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-methylphenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethylamino]-[1,2,4]triazolo[1,5-aJpyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[N-(2,2,2-trifiuoroethyl)-N-(2-methylpropyl)-amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-5 trifluoroethyl)-N-(2-methylpropyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidinet 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-(2-methylpropyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-trifluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-(2-methylpropyl)amino]-['l ,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-methylphenyl)-7-[N-(2,2,2-trif]uoroethyl)-N-(2-methylpropyl)amrno]-10 [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2- trifluoroethyl)-N-methylamino]-[1,2,4]triazolo[1,5-a]pynmidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-methylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-trifluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-methylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-15 methylphenyl)-7-[N-(2,2,2-trifluoroethyl)-N-methylammo]- [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethy))-N-isopropylamino]-[1,2,4]trtazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-isopropylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-trifluorophenyl)-7-[N-(2,2,2-20 trifluoroethyl)-N-isopropylaminoH1,2,4]triazolo[1,5-aJpynmidine, 5-chloro-6-(2-chtoro-6-fIuorophenyl)-7-[N-(2,2,2-tnfluoroethyl)-N-isopropylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-(1-phenylethyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-[N,N-di-(2,2,2-trifIuoroethyl)-amino3-25 [1,2,4]triazolo[1,5-aJpyrimidine, 5-chloro-6-(2-methylphenyl)-7-[N,N-di-(2,2,2-trifluoroethyl)aminoH1,2,4]tnazolo[1,5-a]pynmidine, 5-chloro-6-(2-chlorophenyl)-7-[N,N-di-(2,2,2-trifluoroethyl)-amino]-[1,2,4]triazolo[1,5-aJpyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[N,N-di-(2,2,2-trifIuoroethyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N,N-di-(2,2,2-30 trifluoroethyl)-aminoH1,2,4]triazolo[1,5-a]pyrimidine, 5-ch!oro-6-(2,4,6-trifluorophenyl)-7-tN,N-di-(2,2,2-trifluoroethyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-[N,-(2,2,2-trifluoroethyl)-N-(1,2-dimethylpropyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5- SUBST1TUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 9 chloro-6-(2,4,6-trifluorophenyl)-7-[N,-(2,2,2-trifluoroethyl)-N-(trimethylsilylmethyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-bromo-5-chlorophenyl)-7-[2-(1,1,1-trifluoro)propylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chlorophenyl)-7-(2,2,2-trifluoroethylamino)-5 [1,2,4Jtriazolo[1,5-a]pyrimidine, 5-chloro-6-(4-chlorophenyl)-7-(2,2,2- trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(4-bromophenyl)-7-(2,2,2-trifluoroethylamino)-[1,2,4]triazoio[1,5-a]pyrimidine, 5-chloro-6-(4-methoxyphenyl)-7-(2,2,2-tnfluoroethylamino)-[1,2,4]tnazolot1,5-a]pyrimidine, 5-chloro-6-(4-nitrophenyl)-7-(2,2,2-trifluoroethylamino)-10 [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-fluorophenyl)-7-(1-phenyl-2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[2-( 1,1,1 -trifiuoro)butylamino]-[ 1,2,4]triazolo[ 1,5-a]pyrimidine, 5-chloro-6-(2-chloro-6-fluorophenyl)-7-(1-phenyl-2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pynmidine, 5-chloro-6-(2-fluorophenyl)-7-[2-(1,1,1-15 trifluoro)butylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluorophenyl)-7-(1-phenyl-2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-trifiuorophenyl)-7-(1-phenyl-2,2,2-trifliioroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4,6-trifluoropheriyl)-7-[2-(1,1,1-trifluoro)butylamino]-[1,2,4]triazolo[1,5-a]pynmidine, 5-20 chloro-6-(2,6-difluorophenyl)-7-[2-(1,1,1-trifluoro)butylamino]- [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chlorophenyl)-7-[2-(1,1,1-trifluoro)butylamino]-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2-chlorophenyl)-7-(1-phenyl-2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,4-difluorophenyl)-7-(2,2,2-trifluoroethylamino)-[1,2,4]trrazolo[1,5-a]pyrimidine, 5-25 chloro-6-(2,4,6-trifluorophenyl)-7-[2-(1,1,1 -trifluoro)-3-methylbutylamino]- [1,2,4]triazolo[1,5-a]pyrimidine, 5-chloro-6-(2,6-difluoro-4-methoxyphenyl)-7-[2-(1,1,1-tnfluoro)propylamino]-[1,2,4]triazolo[1,5-a]pyrimidine. The present invention further provides a process for the preparation of a compound of formula I as defined above which comprises 30 treating a compound of the general formula II SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 10 l' in which L1 through L5 and Hal are as defined in any one of the preceding claims, with an amine or amide of the general formula III M Yl —R2 (HI) f,c—ch V, 5 in which R1 and R2 are as defined hereinbefore, M represents a hydrogen atom or a free or complexed metal atom, preferably selected from the group consisting of Li, Na, K, Zn and Cu, 10 to produce a compound of formula I Compounds of formula II are known e g from EP 0 550 113 and are conventionally prepared by reacting 3-amino-1,2,4-triazole with 2-phenyl-substituted malonic acid ester of formula IV, 15 wherein R represents alkyl, under alkaline conditions, preferably using high boiling tertiary amines as for example tri-n-butylamine. The resulting 5,7-dihydroxy-6-phenyltriazolopyrimidines are subsequently treated with a halogenating agent, preferably with a brominating or chlorinating agent, such as phosphorus oxybromide or phosphorus oxychloride, neat or in the 20 presence of a solvent The reaction is suitably carried out at a temperature in the ro' (iv) SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 11 range from 0 °C to 150 °C, the preferred reaction temperature being from 80 "C to 125 °C The reaction between the 5,7-dihalo-6-phenyltriazolopyrimidines of formula II and the amine or amide of formula III is conveniently carried out in the presence 5 of a solvent Suitable solvents include ethers, such as dioxane, diethyl ether and, especially, tetrahydrofuran, halogenated hydrocarbons such as dichloromethane and aromatic hydrocarbons, for example toluene The reaction is suitably carried out at a temperature in the range from 0 °C to 70 °C, the preferred reaction temperature being from 10 °C to 35 °C It is also preferred that the reaction is 10 carried out in the presence of a base. Suitable bases include tertiary amines, such as triethylamme, and inorganic bases, such as potassium carbonate or sodium carbonate Alternatively, an excess of the compound of formula III may serve as a base. The compounds according to the invention may also be obtained by 15 reacting a 7-amino-5-halo-6-phenyltriazolopyrimidine with a trifluoroalkanoic acid or a reactive derivative thereof, in particular with trifluoroacetic acid anhydride, in the presence of a base and subsequent reduction of the resulting trifluoroalkanoic amide. The amines of formula III, wherein M represents a hydrogen atom, are well-20 known in the literature or commercially available or may be prepared analogously to methods that are known per se The amides of formula III, wherein M represents a metal atom are, as a rule, obtained from the corresponding amines (M = hydrogen) by reaction with an alkyl lithium compound optionally followed by a transmetallation reaction 25 Due to excellent activity, the compounds of formula I may be used in cultivation of ail plants where infection by phytopathogenic fungi is not desired, e g. cereals, solanaceous crops, vegetables, legumes, apples, vine The compounds of general formula I have been found to have fungicidal activity. Accordingly, the invention further provides a fungicidal composition which 30 comprises an active ingredient, which is at least one compound of formula I as defined above, and one or more carriers A method of making such a composition is also provided which comprises bnnging a compound of formula I as defined above into association with the carrier(s). Such a composition may contain a single active SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 12 ingredient or a mixture of several active ingredients of the present invention. It is also envisaged that different isomers or mixtures of isomers may have different levels or spectra of activity and thus compositions may comprise individual isomers or mixtures of isomers. 5 A composition according to the invention preferably contains from 0 5% to 95% by weight (w/w) of active ingredient. A carrier in a composition according to the invention is any material with which the active ingredient is formulated to facilitate application to the locus to be treated, which may for example be a plant, seed, soil, or water in which a plant 10 grows, or to facilitate storage, transport or handling A carrier may be a solid or a liquid, including material which is normally a gas but which has been compressed to form a liquid The compositions may be manufactured into e.g emulsion concentrates, solutions, oil in water emulsions, wettable powders, soluble powders, suspension 15 concentrates, dusts, granules, water dispersible granules, micro-capsules, gels, tablets and other formulation types by well-established procedures These procedures include intensive mixing and/or milling of the active ingredients with other substances, such as fillers, solvents, solid carriers, surface active compounds (surfactants), and optionally solid and/or liquid auxiliaries and/or adjuvants. The form 20 of application such as spraying, atomizing, dispersing or pouring may be chosen like the compositions according to the desired objectives and the given circumstances Solvents may be aromatic hydrocarbons, e.g. Solvesso® 200, substituted naphthalenes, phthalic acid esters, such as dibutyl or dioctyl phthalate, aliphatic hydrocarbons, e.g. cyclohexane or paraffins, alcohols and glycols as well as their 25 ethers and esters, e g ethanol, ethyleneglycol mono- and dimethyl ether, ketones such as cyclohexanone, strongly polar solvents such as N-methyl-2-pyrrolidone, or y-butyrolactone, higher alkyl pyrrolidones, e.g. n-octylpyrrolidone or cyclohexylpyrrolidone, epoxidized plant oil esters, e.g. methylated coconut or soybean oil ester and water Mixtures of different liquids are often suitable 30 Solid earners, which may be used for dusts, wettable powders, water dispersible granules, or granules, may be mineral fillers, such as calcite, talc, kaolin, montmorillonite or attapulgite. The physical properties may be improved by addition of highly dispersed silica gel or polymers. Carriers for granules may be porous SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 13 material, e.g. pumice, kaolin, sepiolite, bentonite; non-sorptive earners may be calcite or sand. Additionally, a multitude of pre-granulated inorganic or organic materials may be used, such as dolomite or crushed plant residues Pesticidal compositions are often formulated and transported in a 5 concentrated form which is subsequently diluted by the user before application The presence of small amounts of a earner which is a surfactant facilitates this process of dilution. Thus, preferably at least one carrier in a composition according to the invention is a surfactant For example, the composition may contain at two or more carriers, at least one of which is a surfactant. 10 Surfactants may be nonionic, anionic, cationic or zwitterionic substances with good dispersing, emulsifying and wetting properties depending on the nature of the compound according to general formula I to be formulated Surfactants may also mean mixtures of individual surfactants. The compositions of the invention may for example be formulated as wettable 15 powders, water dispersible granules, dusts, granules, tablets, solutions, emulsifiable concentrates, emulsions, suspension concentrates and aerosols. Wettable powders usually contain 5 to 90% w/w of active ingredient and usually contain in addition to solid inert carrier, 3 to10% w/w of dispersing and wetting agents and, where necessary, 0 to 10% w/w of stabilizer(s) and/or other additives such as penetrants 20 or stickers. Dusts are usually formulated as a dust concentrate having a similar composition to that of a wettable powder but without a dispersant, and may be diluted in the field with further solid carrier to give a composition usually containing 0.5 to 10% w/w of active ingredient Water dispersible granules and granules are usually prepared to have a size between 0.15 mm and 2.0 mm and may be 25 manufactured by a variety of techniques. Generally, these types of granules will contain 0 5 to 90% w/w active ingredient and 0 to 20% w/w of additives such as stabilizer, surfactants, slow release modifiers and binding agents. The so-called "dry flowables" consist of relatively small granules having a relatively high concentration of active ingredient. Emulsifiable concentrates usually contain, in addition to a 30 solvent or a mixture of solvents, 1 to 80% w/v active ingredient, 2 to 20% w/v emulsifiers and 0 to 20% w/v of other additives such as stabilizers, penetrants and corrosion inhibitors. Suspension concentrates are usually milled so as to obtain a stable, non-sedimenting fiowable product and usually contain 5 to 75% w/v active SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 14 ingredient, 0.5 to 15% w/v of dispersing agents, 0.1 to 10% w/v of suspending ' agents such as protective colloids and thixotropic agents, 0 to 10% w/v of other additives such as defoamers, corrosion inhibitors, stabilizers, penetrants and stickers, and water or an organic liquid in which the active ingredient is substantially 5 insoluble; certain organic solids or inorganic salts may be present dissolved in the formulation to assist in preventing sedimentation and crystalization or as antifreeze agents for water Aqueous dispersions and emulsions, for example compositions obtained by diluting the formulated product according to the invention with water, also lie within 10 the scope of the invention. Of particular interest in enhancing the duration of the protective activity of the compounds of this invention is the use of a carrier which will provide slow release of the pesticidal compounds into the environment of a plant which is to be protected. The biological activity of the active ingredient can also be increased by 15 including an adjuvant in the spray dilution. An adjuvant is defined here as a substance which can increase the biological activity of an active ingredient but is not itself significantly biologically active. The adjuvant can either be included in the formulation as a coformulant or carrier, or can be added to the spray tank together with the formulation containing the active ingredient 20 As a commodity the compositions may preferably be in a concentrated form whereas the end user generally employs diluted compositions The compositions may be diluted to a concentration down to 0.001% of active ingredient The doses usually are in the range from 0 01 to 10 kg a i./ha. (mixture containing calcium alkyl aryl sulfonate, fatty alcohol ethoxylates and light aromatics / mixture containing calcium alkyl aryl sulfonate, fatty alcohol ethoxylates and light aromatics) SUBSTITUTE SHEET (RULE 26) Examples of formulations according to the invention are. 25 Emulsion Concentrate (EQ Active Ingredient Compound of Example 8 Emulsifier(s) Atlox® 4856 B / Atlox® 4858 B 1> 30 % (w/v) 5 % (w/v) Printed from Mimosa WO 98/46608 PCT/US98/05615 15 Solvent Shellsol®A2) to 1000 ml (mixture of C9 - C10 aromatic hydrocarbons) Suspension Concentrate fSC) Active Ingredient Compound of Example 8 Dispersing agent Soprophor® FL 3) (polyoxyethylene polyaryl phenyl ether phosphate amine salt) Antifoaming agent Rhodorsil® 422 3) (nonionic aqueous emulsion of polydimethylsiloxanes) Structure agent Kelzan® S 4) (Xanthan gum) Antifreezing agent Propylene glycol Biocidal agent Proxel®5) (aqueous dipropylene glycol solution containing 20% 1,2-benisothiazolin-3-one) Water Wettable Powder (\NP) Active Ingredient Compound of Example 8 Atlox® 4995 1) (polyoxyethylene alkyl ether) Witcosperse® D-60 6) (mixture of sodium salts of condensed naphthalene sulfonic acid and alkylarylpolyoxy acetates Carrier/Filler Kaolin Wetting agent Dispersing agent 50 % (w/v) 3 % (w/v) 02% (w/v) 0.2 % (w/v) 5 % (w/v) 0 1 % (w/v) to 1000 ml 60 % (w/w) 2 % (w/w) 3 % (w/w) 35 % (w/w) SUBSTITUTE SHEET (RULE 25) Printed from Mimosa WO 98/46608 16 PCT/US98/05615 Water Dispersible Granules (\NG) Active Ingredient Compound of Example 8 50 % (w/w) Dispersing / Witcosperse® D-4506) 8 % (w/w) Binding agent (mixture of sodium salts of condensed naphthalene sulfonic acid and alkyl sulfonates) Wetting agent Morwet® EFW6> 2 % (w/w) (formaldehyde condensation product) Antifoaming agent Rhodorsil® EP 6703 3) 1 % (w/w) (encapsulated silicone) Disintegrant Agrimer® ATF7) 2 % (w/w) (cross-linked homopolymer of N-vinyl-2-pyrrolidone) Carrier I Filler Kaolin 35 % (w/w) commercially available from ICI Surfactants 2) commercially available from Deutsche Shell AG commercially available from Rhone-Poulenc 5 commercially available from Kelco Co 5) commercially available from Zeneca 6) commercially available from Witco 7) commercially available from International Speciality Products 10 The compositions of this invention can also comprise other compounds having biological activity, e g. compounds having similar or complementary pesticidal activity or compounds having plant growth regulating, fungicidal or insecticidal activity. These mixtures of pesticides can have a broader spectrum of activity than the compound of general formula I alone. Furthermore, the other 15 pesticide can have a synergistic effect on the pesticidal activity of the compound of general formula I The other fungicidal compound can be, for example, one which is also capable of combating diseases of cereals (e.g. wheat) such as those caused by SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 17 Erysipha, Puccmia, Septoria, Gibberella and Helminthosponum spp., seed and soil borne diseases and downy and powdery mildews on vines, early and late blight on solanaceous crops, and powdery mildew and scab on apples etc These mixtures of fungicides can have a broader spectrum of activity than the compound 5 of general formula I alone. Furthermore, the other fungicide can have a synergistic effect on the fungicidal activities of the compound of general formula I Examples of the other fungicidal compounds are anilazine, azoxystrobin, benalaxyl, benomyl, bethoxazin, binapacryl, bitertanol, blasticidin S, Bordeaux mixture, bromuconazole, bupirimate, captafol, captan, carbendazim, carboxin, 10 carpropamid, chlorbenzthiazon, chlorothalonil, chlozolinate, copper-containing compounds such as copper oxychloride, and copper sulfate, cycloheximide, cymoxanil, cypofuram, cyproconazoie, cyprodinil, dichlofluanid, dichlone, dichloran, diclobutrazol, diclocymet, diclomezine, diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, diniconazole, dinocap, ditalimfos, 15 dithianon, dodemorph, dodine, edifenphos, epoxiconazole, etaconazole, ethirimol, etridiazole, famoxadone, fenapanil, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenpiclonil, fenpropidin, fenpropimorph, fentin, fentin acetate, fentin hydroxide, ferimzone, fluazinam, fludioxonil, flumetover, fluquinconazole, flusilazole, flusulfamide, flutolanil, flutriafol, folpet, fosetyt-aluminium, fubendazole, 20 furalaxyl, furametpyr, guazatme, hexaconazole, imazalil, iminoctadine, ipconazole, iprodione, isoprothiolane, kasugamycin, kitazin P, kresoxim-methyl, mancozeb, maneb, mepanipyrim, meproml, metalaxyl, metconazole, methfuroxam, myclobutanil, neoasozin, nickel dimethyldithiocarbamate, nitrothalisopropyl, nuanmol, ofurace, organo mercury compounds, oxadixyl, oxycarboxin, 25 penconazole, pencycuron, phenazineoxide, phthalide, polyoxin D, polyram, probenazole, prochloraz, procymidione, propamocarb, propiconazole, propineb, pyrazophos, pyrifenox, pyrimethanil, pyroquilon, pyroxyfur, quinomethionate, quinoxyfen, quintozene, spiroxamine, SSF-126, SSF-129, streptomycin, sulfur, tebuconazole, tecloftalame, tecnazene, tetraconazole, thiabendazole, 30 thifluzamide, thiophanate-methyl, thiram, tolclofosmethyl, toiylfluanid, triadimefon, triadimenol, triazbutil, triazoxide, tricyclazole, tridemorph, tnflumizole, trifonne, triticonazole, validamycin A, vinclozolin, XRD-563, zarilamid, zineb, ziram SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 18 In addition, the co-formulations according to the invention may contain at least one compound of formula I and any of the following classes of biological control agents such as viruses, bacteria, nematodes, fungi, and other microorganisms which are suitable to control insects, weeds or plant diseases or 5 to induce host resistance in the plants. Examples of such biological control agents are Bacillus thunngiensis, Verticilhum lecanii, Autographica califomica NPV, Beauvana bassiana, Ampelomyces quisquahs, Bacilis subtilis, Pseudomonas chlororaphis, Pseudomonas fluorescens, Steptomyces gnseoviridis and Trichoderma harzianum. 10 Moreover, the co-formulations according to the invention may contain at least one compound of formula I and a chemical agent that induces the systemic acquired resistance in plants such as for example nicotinic acid or derivatives thereof or BION The compounds of general formula I can be mixed with soil, peat or other 15 rooting media for the protection of the plants against seed-borne, soil-borne or foliar fungal diseases. The invention still further provides the use as a fungicide of a compound of the general formula I as defined above or a composition as defined above, and a method for combating fungus at a locus, which comprises treating the locus, which 20 may be for example plants subject to or subjected to fungal attack, seeds of such plants or the medium in which such plants are growing or are to be grown, with such a compound or composition. The present invention is of wide applicability in the protection of crop and ornamental plants against fungal attack. Typical crops which may be protected 25 include vines, grain crops such as wheat and barley, rice, sugar beet, top fruit, peanuts, potatoes, vegetables and tomatoes. The duration of the protection is normally dependent on the individual compound selected, and also a variety of external factors, such as climate, whose impact is normally mitigated by the use of a suitable formulation. 30 The following examples further illustrate the present invention It should be understood, however, that the invention is not limited solely to the particular examples given below. SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/0S61S 19 Example 1 5-Chloro-6-(2-chloro-6-fluorophenyl)-7-N-(2,2,2-trifluoroethylamino)-1,2,4-triazolo[1 5a]pyrimidine A mixture of 2,2,2-trifluoroethylamine (4.2 mmoles) and dichloromethane 5 (10 ml) is added to a mixture of 5,7- dichloro-6-(2-chloro-6-fluorophenyl)-1,2,4-triazolo[1 5a]pyrimidine (1 4 mmoles) and dichloromethane (30 ml) under stirring The reaction mixture is stirred 16 hours at room temperature, subsequently washed two times with 1 N hydrochloric acid and once with water. The organic layer is separated, dried with anhydrous sodium sulfate and the solvent is 10 evaporated under reduced pressure. Treatment of the resulting light brown oil with tert -butyl methyl ether (50 ml) yields beige crystals having a melting point of 194-197 °C. Examples 2-69 15 The following examples (Table I, structure and melting point) are synthesized analogously to Example 1. SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 20 PCT/US98/05615 Exam pie R1 R2 L' L2 L3 L4 L5 melting point (° C) 2 h h ci h h h h 165 3 h h f h f h f 195 4 h h f h h h h 180 5 h h f h h h f 137 6 ch3 h ci h h h f 165-176 7 ch3 h f h h h f 166-167 8 ch3 h f h f h f 184-185 9 ch3 h ch3 h h h h 149-151 10 ch3 h f h h h h 128-130 11 ch3 h ci h h h h 129-130 12 h ally! f h f h f 104-105 13 h ally! ci h h h f 145-146 14 h allyl f h h h h 128 15 h allyl f h h h f 109-111 16 h allyl ci h h h h 129-130 17 h allyl ch3 H h h h 123-130 18 h ethyl f h h h h 136-139 19 h ethyl f h h H f 164-166 20 H ethyl f h f h f 133-134 21 h ethyl ci h h h f 199-202 22 h ethyl ci h h H h 150-158 23 H ethyl ch3 h h h h 174-178 24 h 2-methylpropyl ci h h h f 175 25 h 2-methylpropyl f h h h f 154-155 26 h 2-methylpropyl f h h h h 144 27 h 2-methylpropyl f h f h f 133-134 28 h 2-methylpropyl CO x o h h h H 154-155 29 h methyl f h h H h 142-143 30 h methyl f H h h f 175-177 31 h methyl f h f h f 163 32 H methyl f H h h ci 178-180 33 H methyl ch3 h h h h 147-149 SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 34 h isopropyl f h h h f 147-150 35 h isopropyl f h h h ci 178-183 36 h isopropyl f h f h f 154-158 37 h isopropyl f h h h h 167-170 38 h 1-phenylethyl f h h h h oil 39 h 2,2,2-tnfluoroethyl ci h h h h 212-213 40 h 2,2,2-tnfluoroethyl ch3 h h h h 223-226 41 h 2,2,2-trifiuoroethyl f h h h h 185-186 42 h 2,2,2-trifluoroethyl f h h h ci 234-237 43 h 2,2,2-tnfluoroethyl f h h h f 208-210 44 h 2,2,2-tnfluoroethyl f h f h f 177-179 45 h 1,2-dimethylpropyl f h h h f 154-158 46 h tnmethylsilylmethyl f h f h f 85 47 ch3 methyl Br h h ci h 160-169 48 h h h h ci h h 170 49 h h h h Br h h 176-177 50 h h h h och3 h h 183-185 51 h h h h no2 h h 237 52 c8h5 h f h h h h 114 53 c2h5 h f h h h ci 162 54 c6h5 h f h h h ci 108 55 C2hs h f h h h h 133 56 cahs h f h h h f 148 57 c8h5 h f h f h f - 86 58 c,h5 h f h f H f 177 59 c2h5 h f h f H f 171 60 c2h5 h ci h h h h oil 61 c,h5 h ci h h h h oil 62 h h f h f h h 181 63 i-c3h7 h f h f h f 104 64 h h f h och3 h f oil 65 H h f h h h Br 187 66 ch3 h f h h h Br 184-185 67 h h f f h h f 183 68 ch, h f f H h f 149 SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 22 69 H H F F F F F oil Biological Investigations A. Determination of Minimum Inhibitory Concentration by Test Compounds in the Serial Dilution Test with Various Phytopathogenic Fungi 5 The MIC (Minimum inhibitory Concentration) value, which indicates the lowest concentration of the active ingredient in the growth medium which causes a total inhibition of myecelial growth, is determined by serial dilution tests using Microtiter plates with 24 or 48 wells per plate. The dilution of the test compounds in the nutrient solution and the distribution to the wells is earned out by a TECAN 10 RSP 5000 Robotic Sample Processor. The following test compound concentrations are used: 0.05, 0.10, 0.20, 0.39, 0.78, 1.56, 3 13, 6.25, 12.50, 25.00, 50.00 and 100 00 mg/ml For preparation of the nutrient solution, V8 vegetable juice (333 ml) is mixed with calcium carbonate (4 95 g), centrifuged, the supernatant (200 ml) diluted with water (800 ml) and autoclaved at 121 °C for 30 mm. 15 The respective inocula (Altemana solani, ALTESO; Botrytis cinerea, BOTRCI; Leptosphaena nodorum, LEPTNO; Phytophthora mfestans, PHYTIN, Magnaporthe grisea f. sp. oryzae, PYRIOR, Pyrenophora teres, PYRNTE; Rhizoctonia solani, RHIZSO,) are added into the wells as spore suspensions (50 ml; 5x10s/ml) or agar slices (6 mm) of an agar culture of the fungus 20 After 6-12 days incubation at suitable temperatures (18-25°C), the MIC values are determined by visual inspection of the plates (Table II; n. t = not tested). SUBSTITUTE SHEET (RULE 26) Printed from Mimosa 1 2 3 6 7 8 9 10 11 12 13 15 16 19 20 27 30 31 46 47 49 53 55 56 57 59 60 PCT/US98/05615 23 Table II alteso botrci leptno phytin pyrior pyrnte rhiszo 3.13 1.56 6.25 12.5 0.78 6.25 6 25 12.5 6 25 50 125 0.78 12.5 25 1 56 1.56 6.25 25 0.2 6.25 6.25 3.13 125 25 > 100 3.13 25 6 25 1.56 25 50 > 100 0.78 125 6 25 0.78 3.13 3.13 > 100 0.78 6.25 3 13 25 25 12.5 > 100 3.13 > 100 12 5 6.25 > 100 50 25 1 56 > 100 12 5 3 13 6.25 25 100 0.39 6.25 6.25 0 39 0 78 3.13 > 100 0 04 3.13 0 78 3.13 3.13 > 100 > 100 0.1 > 100 1 56 1.56 1.56 6.25 > 100 004 6 25 1.56 1.56 6 25 12.5 > 100 0.39 50 50 0.78 1.56 > 100 > 100 0.04 > 100 0.78 0.78 0.78 3.13 > 100 0 04 1 56 0.78 0.2 02 0.39 > 100 0 04 > 100 3.13 3.13 12.5 > 100 > 100 0.78 25 > 100 0.78 3.13 50 > 100 0 1 12 5 1.56 0.78 6.25 > 100 25 1.56 25 > 100 12.5 12.5 25 > 100 1 56 > 100 50 12.5 25 50 100 0.78 25 50 6.25 12.5 > 100 > 100 1.56 > 100 > 100 3 13 125 50 > 100 1.56 > 100 > 100 3.13 12 5 > 100 > 100 1.56 3.13 > 100 50 > 100 > 100 > 100 0.78 100 > 100 6.25 12.5 25 >100 0.39 > 100 6 25 3 13 25 25 25 1 56 25 25 0.39 1 56 1.56 100 0 04 6.25 12 5 SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 24 Ex No ALTESO BOTRCI LEPTNO PHYTIN PYRIOR PYRNTE RHISZO standard * 125 125 100 > 100 50 50 100 * 5-Chloro-6-(2-chlorophenyl)-7-N-ethylamino-1,2,4-triazolo[1 5a]pyrimidine has been used as standard, this compound corresponds to the compound of example 2, in which the 7-(2,2,2-trifluoroethyl)amino group has been replaced by an 5 ordinary 7-ethylamino group. B. Determination of residual control of grape powdery mildew on vine leaves Method for Evaluation of the compounds of formula I to control powdery mildew on grapes (Uncinula necator) 10 Test plants Cuttings of cultivar Muller-Thurgau were grown in the greenhose at temperatures between 18 °C and 25 °C and 50 to 70 % relative humidity. When 6 to 8 leaves had developed the plants were cut back to 3 - 4 equally sized leaves. Plants were cultivated in pots containing FLORAGAD as a substrate. 15 Application Three to four plants per treatment were used. Application of the compounds of formula I was carried out 3 days before infection in the prophylactic tests. The test plants were sprayed to run off in a spray cabinett using 20 ml of spray wash The compounds of formula I were dissolved in acetone at a concentration of 0 5 % 20 The stock solution was diluted wrth water to give the final concentrations. Formulated fungicides were also diluted with water prior to application. Infection The plants were artificially infected with conidia of Uncinula necator by dusting spores from freshly sporulating grape leaves from the Uncinula necator stock 25 culture over the test plants The spores were allowed to settle on the leaves for 1 hour. The plants remained in the greenhouse without additional light at temperatures between 16 °C and 30 "C for 24 hours Evaluation Evaluation was carried out 21 days after infection by assessing the percentage of 30 infected leaf area of each of the 4 treated leaves. The activity in % was calculated using the ABBOTT formula' SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 25 % infection in treated % activity = 100 % infection in untreated The results of this evaluation are shown in Table III' Table III Uncmula necator on Vines Example No. Rate (ppm a.i.) Efficacy (%) 3 25 100 12.5 100 6.25 100 3.13 91 2 25 38 12.5 19 6.25 5 3 13 0 8 25 100 12.5 100 6.25 100 3.13 97 standard * 25 5 12 5 11 6.25 2 3.13 0 5 * The same compound as in the investigations regarding the MIC values has been used as standard C. Foliar Systemicity C-1 Grape variety Muller-Thurgau 10 PATHOGEN-Uncinula necator TEST PROCEDURE. 1. Grape cuttings are grown in 8 cm diameter plastic in the greenhouse. 2 Formulated compounds are applied to a young fully expanded leaf in a transverse band using an airbrush with a 0 5 mm circular nozzle at an air SUBSTITUTE SHEET (RULE 26) PCT/US98/05615 x 100 Printed from Mimosa WO 98/46608 PCT/US98/05615 26 pressure of 500 mbar. The band is sprayed onto the lower leaf surface, perpendicular to the leaf axis using a cardboard mask with a 5-mm wide slit. The location of the band is marked on the upper leaf surface using a permanent marker and is typically 4 cm from the leaf apex. After application, 5 the plants are not moved until the bands are dry 3. After treated plants have dried, they are moved to the greenhouse and kept there for 2 days to allow for movement of the compounds The plants are maintained with bottom watering 4 Two days after application, the grape plants are inoculated by dusting them 10 with powdery mildew conidia in the greenhouse. Sporulating diseased leaves from stock culture plants are brushed with a brush in the air over the test plants so that the conidia can settle onto the upper leaf surfaces of the test plants. Evaluations are made 12-14 days after inoculation. 15 (>2 Wheat Powdery Mildew (WPM): HOST Wheat (Triticum aestivum L.) variety Kanzler PATHOGEN Ervsiphe graminis DC. f.sp tntici E Marchal TEST PROCEDURE: 1 Wheat seed (8/pot) is planted in 8 cm diameter plastic pots in the greenhouse 20 2. When the primary leaf is fully expanded, the plants are cut back to four in each pot of which two are marked with a permanent marker 5 cm below the leaf tip on the upper leaf surface Thus there are two band-treated and two untreated plants in each pot. 3. A pipette is used to apply 5 |j| of the formulated compound in a band on the 25 lower leaf surface opposite the mark. The application band should cover the whole leaf width After application, the plants are not moved until the bands are dry (half an hour or so later). 4 After treated plants have dried, they are moved to the greenhouse and kept there for 2 days to allow for movement of the compounds The plants are 30 maintained with bottom watering. 5. Two days after application, the plants are inoculated by dusting them with powdery mildew conidia in the greenhouse Evaluations are made 7-8 days SUBSTITUTE SHEET (RULE 25) Printed from Mimosa WO 98/46608 PCT/US98/05615 27 after inoculation. Alternatively, plants are inoculated with Puccinia recondita (wheat leaf rust pathogen) and evaluations made 7-8 days thereafter Evaluation Three types of compound movement are assessed by evaluating disease in three 5 areas of each band-treated leaf. Translaminar movement: The percent disease area is assessed for the translaminar band area (marked area of the upper leaf surface directly opposite where band was applied on the lower leaf surface, width of band approximately 5 mm). Translaminar disease control is then calculated using the following formula' % disease in treated plants % disease control = 100 - x 100 10 % disease in untreated plants Distal movement and proximal movement. The distal and proximal disease-free zones on the upper leaf surface are measured in mm. The distal direction is from the band toward the leaf apex and the proximal direction is from the band toward 15 the leaf base. The percent of the disease-free zone relative to the entire distance between the band and leaf apex or base is calculated (for Grape 40 mm equals 100%) If disease is noticeably lighter in the distal or proximal area this is also noted. 20 FORMULATION AND CONTROLS: 1 The compounds are formulated in a solvent/surfactant system consisting of 5% acetone and 0 05% Tween 20 in deionized water. Compounds are dissolved in acetone prior to dilution with Tween water. Formulated compounds are prepared using deionized water. Compounds are typically 25 tested at 400 ppm. 2. Three kinds of controls are included. Plants band-treated with the solvent/surfactant solution and inoculated (Solvent Blank) Untreated plants which are inoculated (Inoculated Control). 30 The results of this evaluation are shown in Table IV, in which the diseases have been abbreviated as follows: SUBSTITUTE SHEET (RULE 26) Printed from Mimosa WO 98/46608 PCT/US98/05615 28 Wheat powdery mildew WPM Grape powdery mildew GPM Wheat leaf rust WLR Table IV Foliar Systemicity Ex. No. Disease Proximal Distal Movement Translaminar Movement (mm (mm from band) Activity ( % ) from band) 1 WPM 3 43 TOO GPM 6 50 100 WLR 5 48 100 ' 2 GPM ' ' "8" " 36 100" WLR 4 21 100 "3 GPM 7 50 "'100 WLR 4 23 100 " " 4 GPM 7 32 100 WLR 3 6 100 Standard2 GPM 2 6 100 WLR 4 8 100 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2-chloro-6-fluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine which is disclosed in US patent no. 5,593,996 has been used as standard2 SUBSTITUTE SHEET (RULE 26) Printed from Mimosa i ii -29- </div>

Claims

<div class="application article clearfix printTableText" id="claims"> claim?;

1. A compound of the general formula I in which R1 and R2 each independently represent a hydrogen atom or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl or phenyl group, Hal represents a halogen atom L1 through L5 each independently represent an hydrogen or halogen atom or an alkyl, aikoxy or nitro group in which the terms alkyl, alkenyl, alkynyl alkadienyl refer to straight or branched chain radicals or moieties having up to 10 carbon atoms; in which each optionally substituted group independently is substituted by one or more halogen atoms or nitro, cyano, alkyl, cycloalkyi, cycloalkenyl, haloalkyl, halocycloalkyl, aikoxy, haloalkoxy, trialkylsilyl, phenyl, halo- or dihalo-phenyl or pyridyl groups.

2. A compound according to Claim 1 in which at least one of L1 and L5 represents a halogen atom

3. A compound according to Claim 1 or 2 in which R1 represents hydrogen atom or a methyl group.

4. A compound according to any of the preceding Claims in which R2 represents a hydrogen or a C,.10 alkyl group. INTELLECTUAL PROPERTY OFFICE OF N X. 2 5 MAY 2001 ftECESVED

5. A compound according to any of the preceding Claims in which at least one of R1 and R2 represents a hydrogen atom.

6. The following compounds of formula I: 5-chloro-6-(2-chloro-6-fluorophenyl)-7-(2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-difluorophenyl)-7-(2,2,2-trifluoroethylamino)-[l^.^triazoiofl.S-ajpyrimidine 5-chloro-7-(2,2l2-trifluoroethylamino)-6-{214,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-chlorophenyl)-7-(2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-fluorophenyt)-7-(2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-{2-chloro-6-fluorophenyl)-7-[2-(1,1,'i-trifluoro)propylaminoJ-[1,2,4]triazolo[1,5-a3pyrimidine S-chloro-S-^.S-difluorophenyl^-^-O.I.I-trifluoro^ropylamino]-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2,4,6-trifluorophenyl)-7-[2-(1,1,1-trifluoro)propylaminoJ-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-methylphenyl)-7-[2-(1,1,1 -trifluoro)propylamino]-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-fluorophenyl)-7-[2-(1,1,1-trifluoro)propylaminoj-(1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-chlorophenyl)-7-[2-(1,1,1-trifluoro)propylaminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,4,6-trifluorophenyI)-7-[N-(2,212-trifluoroethyl)-N-allylamino]-[1,2,4]triazoIo[1,5-ajpyrimidine 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[N-(2l2!2-trifluoroethyl)-N-allylamino]-[1,2,4]triazolo[1,5-ajpyrimidine 5-chioro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylaminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylamino]-[1,2.4]triazolo[1,5-ajpyrimidine I OFFICE OF NZ. I -9 FEB 2001 i received -31- 50 5-chloro-6-(2-chlorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylaminoj-[1,2,4]triazolo[1,5-3}pyrimidine 5-chloro-6-(2-methylphenyl)-7-[N-(2,2,2-trifluoroethyl)-N-allylaminoj-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethy!)-N-ethylaminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-dif!uoropheny!)-7-[N-(2,2,2-trifluoroethyl)-N-ethylaminoj-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(214,6-trifIuorophenyl)-7-[N-(2,2>2-trifluoroethyl)-N-ethylamino]-[1,2,4]triazolo[1,5-a]pyrimidine 5-chIoro-6-(2-chloro-6-fluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethyIaminoj-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-chlorophenyl)-7-[N-(2.2,2-tnfluoroethyl)-N-ethylaminoj-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-methyJphenyl)-7-[N-(2,2,2-trifluoroethyl)-N-ethylaminoj-[1,2,4Jtriazo!o[1,5-ajpyrimidine 5-chloro-6-(2-chloro-6-f!uorophenyl)-7-[N-(2,212-trifluoroethyl)-N-(2-methylpropyl)aminoj-[1,2,4Jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2,6-difIuorophenyl)-7-[N-(2,2,2-trifluoroethyI)-N-(2-methyipropyl)aminoj-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2-fluorophenyl)-7-(N-(2,2,2-trifluoroethyl)-N-(2-methylpropyl)-amino]-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2,4,6-trifluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-(2-methylpropyl)aminoj-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro6-(2-methylphenyl)-7-[N-(2,2,2-trifluoroethyl)-N-(2-methylpropyl)-aminoJ-[1,2t4jtriazolo[1,5rajpyrimidine 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifIuoroethyl)-N-methylaminoj-[1,2,4Jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2,6-difIuorophenyl)-7-[N-(2J2,2-trifluoroethyl)-N-methylaminoj-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2,4,6-trifluorophenyl)-7-[N-(2,212-trifluoroethyl)-N-methylaminoj-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2-methyIphenyl)-7-[N-(2,2,2-tr'rfluoroethyl)-N-methylaminoj-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2-fluorophenyl)-7-[N-(2,2,2-trifluoroethyi)-N-isoprop 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-isopropylamino]-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2l4,6-trifluorophenyl)-7-[N-(2,212-trifluoroethyl)-N-isopropylamino]-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[N-(2,2,2-trifliioroethyl)-N-isopropylamino]-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-difluorophenyl)-7-[N-(2,2,2-trifluoroethyl)-N-(1-phenylethyOaminoj-n^^jtriazolofl ,5-ajpyrimidine 5-chloro-6-(2-fluorophenyl)-7-[N,N-di-(2,2,2-trifluoroethyl)aminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-methylphenyl)-7-[N,N-di-(2,2l2-trifluoroethyl)amino]-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-chlorophenyl)-7-[N,N-di-(2,2,2-trifluoroethyl)amino]-J [1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-chloro-6-fluorophenyI)-7-[N,N-di-(2,2,2-trifluoroethyl)aminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-difluorophenyl)-7-[N,N-di-(2,2,2-trifluoroethyl)aminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,4l6-trif!uorophenyl)-7-[N,N-di-(2,2,2-trifluoroethyl)amino]-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-difluorophenyl)-7-[Nl-(2,2,2-trifluoroethyl)-N-(1,2-dimethylpropyl)aminoj-[1,2,4]triazolo(1,5-ajpyrimidine 5-chloro-6-{2,4I6-trif[uorophenyi)-7-[N,-(2,2<2-trifluoroethyl)-N-(trimethylsi!ylmethyl)amino]-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-bromo-5-chlorophenyl)-7-[2-(1l1,1-trif!uoro)propylamino]-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2-chlorophenyl)-7-{2,2,2-trifluoroethylamino)-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(4-chlorophenyl)-7-{212,2-trifluoroethylamino)-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(4-bromophenyl).-7-(2,2,2-trifluoroethylamino)-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(4-methoxyphenyl)-7-(2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(4-nitrophenyl)-7-(2,2r2-trifluoroethylamino)- . [1,2,4jtriazolo[1,5-ajpyrimidine I ,nteJ;LJCtual property I office of n.z. I - 9 FEB 2001 i received -33- 50 0 1 43 5-chloro-6-(2-fluorophenyl)-7-(1-phenyl-2,2,2-trif]uoroethylamino)- . .. [1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-chloro-6-fluorophenyl)-7-[2-(1,1,1-trifluoro)butylaminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-chloro-6-fluorophenyl)-7-(1-phenyl-2,2,2-trifluoroethylamino)-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2-fluorophenyl)-7-[2-( 1,1,1 -trifluoro)butylaminoj-[1,2.4]triazolo[l ,5-a]pyrimidine 5-chloro-6-(2,6-difluorophenyl)-7-(1-phenyl-2,2,2-trifluoroethylamino)-[l^^jtriazolofl.S-ajpyrimidine S-chloro-S-^AS-trifluorophenyO^-O-phenyl^^^-trifluoroethylamino)-[1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2,4,6-trifluorophenyl)-7-[2-(1,1,1-trifluoro)butylaminoj-[1,2,4]triazolo[1,5-a]pyrimidine 5-chloro-6-(2,6-difluoropheny[)-7-[2-(1.1,1-trifluoro)butylamino]-[1.2,4jtriazolo[1,5-a]pyrimidine 5-chloro-6-(2-chlorophenyl)-7-[2-(1.1,1-trifluoro)butylaminoj-[1,2,4]triazo[o[1,5-ajpyrimidine 5-chloro-6-(2-chlorophenyl)-7-(l-pnenyl-2,2,2-trifluoroethylamino)-[1,2,4Jtriazolo[1,5-ajpyrimfdine 5-chloro-6-(214-difluorophenyl)-7-(2,2,2-trifluoroethylamino)-(1,2,4]triazolo[1,5-ajpyrimidine 5-chloro-6-(2,4,6-trifIuorophenyl)-7-[2-(1,1,1 -trifluoro)-3-methylbutylaminoj-[1,2,4jtriazolo[1,5-ajpyrimidine 5-chloro-6-(2,6-difluoro-4-methoxyphenyl)-7-[2-(1,1 ,l-trifluoro)propylaminoj-[1,2,4]triazolo[1,5;rajpyrimidine.

7. A process for the preparation of a compound of formula I as defined in any one of the preceding claims which comprises treating a compound of the general formula II intellectual property OFFICE OF N.Z - 9 FEB 2001 received *N Hal in which L1 through L5 and Hal are as defined in any one of the preceding claims; with an amine of the general formula M N —R (III) FaC—CH 3 \ . in which R1 and R2 are as defined in any one of the preceding claims, M represents a hydrogen atom or a free or complexed metal atom, to produce a compound of formula I.

8. A fungicidal composition which comprises a carrier, and as active agent, at least one compound of formula I as defined in any one of Claims 1 to 6.

^ 9. A method of combating phytopathogenic fungus at a locus which comprises treating the locus with a compound of formula I as defined in any one of Claims 1 to 6 or with'a composition as defined in Claim 8.

10 The use as a fungicide of a compound of formula I as defined in any one of Claims 1 to 6 or a composition as defined in Claim 8. I -9 FEB 2001 [ RECEIVED j[| -35- oo

11. A compound of general formula I as defined in Claim 1 substantially as herein described with reference to any example thereof.

12. Compounds of formula I as claimed in Claim 6 substantially as herein described with reference to any example thereof.

13. A process for the preparation of a compound of formula I as claimed in claim 7 substantially as herein described with reference to any example thereof

14. A fungicidal composition as claimed in claim 8 substantially as herein described with reference to any example thereof.

15. A method of combating phytopathogenic fungus at a locus as claimed in claim 9 substantially as herein described with reference to any example thereof. 16 The use as claimed in claim 10 substantially as herein described with reference to any example thereof. I \LIBRARY\TVG\CLAIMS\414300 WPD END </div>